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苜蓿中华根瘤菌 1021 中 Δ9 脂肪酸去饱和酶的生化和分子证据。

Biochemical and molecular evidence of a Δ9 fatty acid desaturase from Ensifer meliloti 1021.

机构信息

Departamento de Biología Molecular, Facultad de Ciencias Exactas, Físico-Químicas y Naturales, Universidad Nacional de Río Cuarto, CPX5804BYA Río Cuarto, Córdoba, Argentina.

Departamento de Biología Molecular, Facultad de Ciencias Exactas, Físico-Químicas y Naturales, Universidad Nacional de Río Cuarto, CPX5804BYA Río Cuarto, Córdoba, Argentina.

出版信息

Microbiol Res. 2014 May-Jun;169(5-6):463-8. doi: 10.1016/j.micres.2013.08.003. Epub 2013 Sep 5.

Abstract

It has been reported that Ensifer meliloti presents a high proportion of monounsaturated fatty acids and has a putative desaturase gene designated as PhFAD12 (National Centre for Biotechnology Information), encoding a putative Δ12 desaturase-like protein. In this work, we report the desaturation capacity and characterisation of this gene encoding the putative fatty acid desaturase of E. meliloti 1021. This gene was also isolated from the rhizobial strain and overexpressed in Escherichia coli. Compared to a control, the expression of this gene in the transformed strain decreased the levels of palmitic and stearic acids, enhanced palmitoleic and cis-vaccenic levels, and allowed for the detection of oleic acid. E. coli overexpressing the putative desaturase gene was capable of desaturating palmitic and stearic acids to monounsaturated fatty acids, similarly to the rhizobial strain. Our studies show that AAK64726 encodes a Δ9 desaturase instead of a Δ12 desaturase as previously indicated. This work describes evidence for the presence of a desaturase-mediated mechanism in monounsaturated fatty acid synthesis in E. meliloti 1021, which is modified by high growth temperature. This mechanism supplements the anaerobic mechanism for unsaturated fatty acid synthesis.

摘要

据报道,根瘤固氮螺菌(Ensifer meliloti)含有较高比例的单不饱和脂肪酸,并具有一个假定的去饱和酶基因,命名为 PhFAD12(美国国家生物技术信息中心),编码一个假定的Δ12 去饱和酶样蛋白。在这项工作中,我们报告了根瘤固氮螺菌 1021 中编码假定脂肪酸去饱和酶的基因的去饱和能力和特性。该基因也从根瘤菌株中分离出来,并在大肠杆菌中过表达。与对照相比,该基因在转化菌株中的表达降低了棕榈酸和硬脂酸的水平,增加了棕榈油酸和顺式芸苔酸的水平,并检测到油酸。过表达假定去饱和酶基因的大肠杆菌能够将棕榈酸和硬脂酸不饱和化为单不饱和脂肪酸,这与根瘤菌株相似。我们的研究表明,AAK64726 编码的是一个 Δ9 去饱和酶,而不是先前表明的 Δ12 去饱和酶。这项工作描述了根瘤固氮螺菌 1021 中存在一种通过去饱和酶介导的机制来合成单不饱和脂肪酸的证据,这种机制在高生长温度下被修饰。这种机制补充了厌氧机制合成不饱和脂肪酸。

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